Canonical Allele Identifier: CA1364835856

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403238C= , CM000665.2:g.52403238C=	GRCh38
NC_000003.11:g.52437254C= , CM000665.1:g.52437254C=	GRCh37
NC_000003.10:g.52412294C=	NCBI36
NG_031859.1:g.11756G= , LRG_529:g.11756G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1790G= MANE Select	ENSP00000417132.1:p.Ser597=
ENST00000296288.9:c.1736G=	ENSP00000296288.5:p.Ser579=
ENST00000460680.5:c.1790G=	ENSP00000417132.1:p.Ser597=
ENST00000466093.1:n.197G=
ENST00000469613.5:c.120-397G=
ENST00000478368.1:c.293G=	ENSP00000420647.1:p.Ser98=
NM_004656.3:c.1790G=	NP_004647.1:p.Ser597=
XM_011534149.1:c.1790G=	XP_011532451.1:p.Ser597=
XM_011534150.1:c.1790G=	XP_011532452.1:p.Ser597=
XM_011534151.1:c.1736G=	XP_011532453.1:p.Ser579=
XM_011534152.1:c.1790G=	XP_011532454.1:p.Ser597=
XM_011534149.3:c.1790G=	XP_011532451.1:p.Ser597=
XM_011534150.3:c.1790G=	XP_011532452.1:p.Ser597=
XM_011534151.3:c.1736G=	XP_011532453.1:p.Ser579=
XM_011534152.2:c.1790G=	XP_011532454.1:p.Ser597=
XM_017007303.2:c.1736G=	XP_016862792.1:p.Ser579=
NM_004656.4:c.1790G= MANE Select	NP_004647.1:p.Ser597=